Roberto Giorda

Bosisio Parini, Italy

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 72 publications

How nature nurtures: prenatal exposure to green space buffers the effects of maternal stress on neonatal BDNF methylation.

How nature nurtures: prenatal exposure to green space buffers the effects of maternal stress on neonatal BDNF methylation.

Journal: Molecular psychiatry

Published: October 20, 2025

Internalizing and Externalizing Traits During Adolescence: Using Epigenetics and Perinatal Risks to Differentiate Clusters of Symptoms.

Internalizing and Externalizing Traits During Adolescence: Using Epigenetics and Perinatal Risks to Differentiate Clusters of Symptoms.

Journal: Biomolecules

Published: July 08, 2025

Constitutional copy number amplifications: rare or under-evaluated? Revisiting a 25-year-old cold case.

Constitutional copy number amplifications: rare or under-evaluated? Revisiting a 25-year-old cold case.

Journal: European journal of human genetics : EJHG

Published: March 11, 2025

A de novo pathogenic variant in MICAL-1 causes epilepsy with auditory features.

A de novo pathogenic variant in MICAL-1 causes epilepsy with auditory features.

Journal: Epilepsia open

Published: February 12, 2024

Alterations in neural activation in the ventral frontoparietal network during complex magnocellular stimuli in developmental dyslexia associated with READ1 deletion.

Alterations in neural activation in the ventral frontoparietal network during complex magnocellular stimuli in developmental dyslexia associated with READ1 deletion.

Journal: Behavioral and brain functions : BBF

Published: December 12, 2023

Clinical phenotype and next-generation sequencing as essential tools for the diagnosis of a rare form of congenital myopathy due to a TRIP4 intragenic deletion.

Clinical phenotype and next-generation sequencing as essential tools for the diagnosis of a rare form of congenital myopathy due to a TRIP4 intragenic deletion.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: August 13, 2023

Sex-dimorphic pathways in the associations between maternal trait anxiety, infant BDNF methylation, and negative emotionality.

Sex-dimorphic pathways in the associations between maternal trait anxiety, infant BDNF methylation, and negative emotionality.

Journal: Development and psychopathology

Published: March 01, 2023

Prenatal exposure to environmental air pollution and psychosocial stress jointly contribute to the epigenetic regulation of the serotonin transporter gene in newborns.

Prenatal exposure to environmental air pollution and psychosocial stress jointly contribute to the epigenetic regulation of the serotonin transporter gene in newborns.

Journal: Molecular psychiatry

Published: February 27, 2023

Maternal and infant NR3C1 and SLC6A4 epigenetic signatures of the COVID-19 pandemic lockdown: when timing matters.

Maternal and infant NR3C1 and SLC6A4 epigenetic signatures of the COVID-19 pandemic lockdown: when timing matters.

Journal: Translational psychiatry

Published: August 17, 2022

Sex-dependent association between variability in infants' OXTR methylation at birth and negative affectivity at 3 months.

Sex-dependent association between variability in infants' OXTR methylation at birth and negative affectivity at 3 months.

Journal: Psychoneuroendocrinology

Published: June 08, 2022

Is Brain-Derived Neurotropic Factor Methylation Involved in the Association Between Prenatal Stress and Maternal Postnatal Anxiety During the COVID-19 Pandemic?

Is Brain-Derived Neurotropic Factor Methylation Involved in the Association Between Prenatal Stress and Maternal Postnatal Anxiety During the COVID-19 Pandemic?

Journal: Frontiers in psychiatry

Published: May 22, 2022

A case of a childhood onset developmental encephalopathy with a novel de novo truncating variant in the Membrane Protein Palmitoylated 5 (MPP5) gene.

A case of a childhood onset developmental encephalopathy with a novel de novo truncating variant in the Membrane Protein Palmitoylated 5 (MPP5) gene.

Journal: Seizure

Published: May 20, 2022

Showing 1-12 of 72

Last Updated: 09/26/2026